내진설계 특수교량의 - AURIC 강의내용 |2007년7월10일(화)| 강습일정및강사 1. 지진입력: 김두기 교수(군산대학교) 1) 장대교량의지진해석을위한지진입력
NMR Basic Principle 노 정 래 군산대학교 2009. 7. 30. Magnetization in the magnetic field...
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Transcript of NMR Basic Principle 노 정 래 군산대학교 2009. 7. 30. Magnetization in the magnetic field...
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NMR BasicNMR Basic Principle Principle
노 정 래군산대학교
2009. 7. 30
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• Magnetization in the magnetic field
• Magnetization under RF pulse
• Detection of Magnetization
• Digitization of FID
• Fourier Transformation
• Experiment Setup
• Chemical shift & Spin coupling constant
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Energy E = h h is Planck constant frequency
nucleus
Spin-0 Spin-1/2 Spin>1/212C, 16O, 18O 1H, 13C, 15N,
19F, 31P
2H, 14N, 17O
- Positive charge
- Magnetogyric ratio,
Magnetic moment,
- spin, I
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I = 1/2
Iz = +1/2
Iz = -1/2
I = 1
Iz = +1
Iz = 0
Iz = -1/2
Z
E = - z Bo = Iz Bo
If magnetic field, Bo is applied to the direction of Z,
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Magnetic moments in the magnetic field, Bo
(one-spin system)
Bo
I=1/2
E = Boh / 2
Bo
: Larmor Frequency
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≡
≡
Mz = Mo
Magnetic moments in the magnetic field, Bo
Mz
Bo
Mx,y
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Bo In the Magnetic field, Bo
- Magnetization, Mo
Mo = Nh2 2 Bo / 4kT
- Precession of Mo at frequency, about the axis of Bo
Bo
The behavior of magnetic moments in the magnetic field, Bo
Equilibrium
Mo
0,
0
yx
z
M
MM
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Bo
= B/2 H = 2.675 108 T-1 rad s-1
(MHz) T (Tesla)
100 2.35
300 7.05
500 11.74
700 16.45
Bo
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nucleus
11.74 T H / Srel Nat.Abd.(%)
1H 500MHz 2.675 1.00 1.00 99.9813C 125.72 0.673 3.977 1.76 10-4 1.1119F 470.39 2.517 1.063 0.83 10015N 50.66 -0.271 9.870 3.85 10-6 0.3731P 202.40 1.083 2.470 0.0665 100
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First NMR Spectra on Water
Bloch, F.; Hansen, W. W.; Packard, M. Bloch, F.; Hansen, W. W.; Packard, M. The nuclear induction experiment.The nuclear induction experiment. Physical Review (1946), 70 474-85. Physical Review (1946), 70 474-85.
11H NMR spectra of waterH NMR spectra of water
Magnetization under RF pulse
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partially correlated spins (Mx,y)
Coherence
coherence
Bo
x
y y
x
x
yy
x
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Spin inversioncoherence
+RF Energy
Equilibrium Non equilibrium
Relaxation
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x
y
z
Mo
rotating frame ( 회전 좌표계 )
x
y
z
Mo
BoBo
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On-resonance Off-resonancex
y
z
Mo
Bo =0
x
y
z
Mo
Bo- /
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2B1sin(+ )
RF wave ( 에너지 )
2B1
B1 ()
xx
B1 ()
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z
x
y
2B1cos(+ )
B1
B
M
My
tp
effect of B1 at (on-resonance)
phase = x
x
y
z
Magnetization in the RF field (phase =0)
Bo = 0
On-resonance
B1 (o)
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Magnetization in the RF field (phase =0)
y
eff eff
effect of B1 at
(off-resonance)
Beff
10 )( iBBkBeff
x
y
z
Mo
Bo - /
B1
Off-resonance
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RF pulse description
2B1cos(+ )
p
B110 )( iBBkBeff
B1 Beff >> Bo – /
pulse
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Mo
x
z
y
Mo
x
z
y
Mo
x
z
y
0,
0
yx
z
M
MM
Mo
x
z
y
0
, 0
MM
M
y
zx
0,
0
yx
z
M
MM
0
, 0
MM
M
x
zy
90x
90y
180x,y
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Mox
z
y
Mo
x
z
y
Mo
x
z
y
90x 180y
1 2 3 4 5
t t
1
Mo
x
z
y
Mo
x
y
1 2
t
3
t
4
z
5
Spin-echo
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Relaxation
Non equilibrium Equilibrium( Mx,y= 0, Mz = M0)
1. Longitudinal (spin-lattice) relaxation : Recovery to Mo
])0([)( 0/
01 MMeMtM ZTt
Z
2. Transverse (spin-spin) relaxation : recovery to Mx,y=0
2/0, )( Tt
yx eMtM Mx,
y
t
tMo
0
> 5 T1
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Magnetization for one spin system
on-resonace)
90x
Coil (induction current)
Signal detection
PPSD
Hz
FID(free induction decay)
Hz
RF
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Mo
x
z
y
90x
(Off-resonace) > o
Summary
x
y
z
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Fourier Transformation (FT)
dtttsidttts
dtetsS ti
)sin()()cos()(
)()(
real imaginary
real imaginary
A() D()
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Hz
Hz
Fourier Transformation (FT)
Real part
Reference frequencyOffset frequency
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FT real imaginary
2/)cos( Tty etM
0
0
0
0
PPSD
2/)sin( Ttx etM
x
y
+
+
0Quadrature Detection
RF
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Scan 1 Scan 2
Relaxation delay (d1)
Pulse width(pw)
Pulse power(tpwr)
Acquisition time (at)
(nt)
Spectral width (sw)
Offset frequency (tof)
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Digitization of FID
PSD
ADC = Analog to Digital Converter
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Digitization of FID
Nyquist frequency
주파수 f 인 주기 함수를 data point 로 나타내기 위한 최소 주파수 , 2f 따라서 한 주기 당 적어도 data point 를 적어도 2 개 이상 얻어야 한다 .
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Real + imaginary data points at simultaneous time (Varian)
sw
npnptat dw 2
np: 총 data point sw: spectral width
In Quadrature detection
npswnp 2
Real part (COS)
Imaginary part (SIN)
160s
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Nyquist Theorem 에 위배
Sampling rate & alias(folding)
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주파수가 1600Hz 인 cos 함수
주파수가 400Hz 인 cos 함수 (alias 함수 )
Nyquist 주파수 :1000Hz
Folding
(aliased)
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Window function
FT
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S/N
61.8
72.0
30.6
122.0
Window Functions
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probe
Experiment Setup
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Locking - 시간에 따른 자장의 변화를 보정 - NMR 용매로 사용하는 deuterium 핵을 이용 - acetone-d6, methanol-d4, chloroform-d, DMSO
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- NMR 시료에 균일한 자장을 만드는 작업- x,y 방향은 spin, z 방향은 shim coil 의 전류량으로 조절- shim 은 NMR 시료 높이에 따라 의존
1. FID 를 이용 한 spin 핵에 대한 FID 이 지수함수로 감소되도록 shim 값을
변화2. Lock level 를 이용 lock level 이 최대가 되도록 shim 값을 변화3. Field gradient 를 이용 (Gradient shimming) field map 에 회귀분석적으로 shim 값 조정
스펙트럼에서 최상의 해상도와 감도를 위해서는 shim 조절이 필수
Shimming
Shimming method
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정상 Z2 감소 후 Z1 재 조정 Z4 감소 후 Z1,Z2 재 조정Z3 감소 후 Z1,Z2 재 조정
Z5 감소 후 Z1,Z2 재 조정
Z3 증가Z4 감소 후 Z1,Z2 재 조정
X, Y, XZ, YZ XY, X2-Y2
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1. Spin2. Temperature setting3. Probe tune (dependence on solvent and temperature)4. Lock & shim5. Adjust reference frequency to the singlet line6. Array pulse width tp
Observer 90o pulse calibration
X
1H ( 13C )
(1H )
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90X 180X
X
BB BB
S (13C)
I (1H)
1/2J 1/2J
Decoupler 90o pulse calibration with IS spin system(e.g. CH)
1. Decoupler 1H 90o calibration
DEPT, Hetcor, INADEQUATE, etc
13C {1H}J
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90X 180X
X
I (1H)
S (13C)
1/2J 1/2J
2. Decoupler 13C 90o calibration
HMQC, HMBC, etc
1H {13C}J
1H-12C
1H-13C
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1H-13C
1H-12C
1H-13C
1H spectrum of 13CH3I
Observer decoupler on-resonance settingTemperature settingTunning -minimize
15N-benzamide
151 Hz
90Hz
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Decoupler field strength(B2) calibration
90X
low-power CW mode
S (13C)
I (1H)
90X
low-power CW mode
I (1H)
S (13C)
B2
B2
JCH
Jr
rJ
JB
CH
2
r 2
13C
1H
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Chemical Shift
1H 1H
Shielding (Screening) factor,
aa
a
b
<
bbfrequency >
600 500 400 300 200 100 MHz
10 9 8 7 6 5 4 3 2 1 0 ppm
HOCH2CH3
CH3CH2
OH
220 200 180 160 140 120 100 80 60 40 20 0
CDCl3
125
CH2CH3
Chemical shift & spin coupling constants
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1H
12 11 10 9 8 7 6 5 4 3 2 1 0
C CH
HC O
HC OHO
CH3O
CH3N
CHCH2
CH3
CH3C
1H and 13C Chemical shifts
(1.15~1.16)
(~0.75)
(1.5~1.6)
13C
220 200 180 160 140 120 100 80 60 40 20 0
C O C
CH3O
CH
CCH3N
CH3
CH2
CH
C OO, N
(13~23)
(22~35)(30~42)
TMS
TMS
ppm
ppm
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alkane
some featured some featured 1313C chemical shiftsC chemical shifts
= -2.3 + 9.1n + 9.4n -2.5 n
CH4 H3C CH3 H2CCH3
CH3HC
CH3
CH3
CH3
-2.3 6.5
16.116.3 24.6
23.3
H2C CH2
alkyne
H2C CH
CH3
H2C CCH3
CH3123.5
115.9
133.4
19.9
111.3
141.8
24.2
HC CH71.9
alkene
arene
128.5 133.3
127.7
125.6
N O
136.0
123.5
149.9143.6
110.4
C C C
H
HH
H
212.6
73.5
CC
CO
OH
170.4
127.2
CH3
CH3
16.5
24.1
H2C
CH2
CH2
CH2
34.128.2
-gauche effect
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Symmetry and Topicity
■ Homotopicity - indistinguishable atoms or groups by symmetry
■ Enantiotopicity - atoms or groups having the mirror image in a molecule
■ Diastereotopicity - atoms or groups not producing the mirror image
H2N COOH
HH
H2 H1
NH2
HHOOC
H1
H2
NH2
HHOOC
H
H1
NH2
HHOOC
CH3
H3C CH3
H
H
HCH3
CH3
CH3HO OH
O O
H H
CH3H3C
HO OH
O O
H3C H
CH3
CH3
H
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Spin-spin coupling(scalar coupling, J-coupling)
Chemical bond (electron colud)
1H 19F 1H 19F
state state
1H
J/2 J/2
J
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- Hybridization of the atoms- Bond lengths- Bond angles and dihedral angles- Substituent effects- The presence of neighboring -bonds
JHH [Hz] sign JCH [Hz] sign JCC [Hz] sign
1J 125-250 + 30-80 +
2J 0-30 -* -10~20 +/- <20 +/-
3J 0-18 + 1-10 + 0-5 +
3+nJ 0-7 +/- <1 +/- <1 +/-
* Usually negative, but sometimes positive
Factors influencing scalar coupling
The order of magnitude and sign of scalar couplings
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Direct coupling ( Direct coupling ( 11J J ))
1JCH= 500 sH3C-CH3 H2C=CH2 C6H6 HC≡CH
1JCH [Hz] 124.9 156.4 158.4 249.0
Hybridization sp3 sp2 sp2 sp
S-fraction 0.25 0.33 0.33 0.5
C C
H
H
F
F
H
C
H
H
H
1JCH= 160.3Hz
Electronegative substituents at the position increase J value
1JCH= 202.2 Hz
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Two-Bond coupling ( Two-Bond coupling ( 22J J ))
The greater the bond angle, more positive is coupling constant
H
H
H
H
H
H
-12.4 Hz
109o120o 120o
-4.5 Hz +2.5 Hz
C
H
C HC
H
H
- 4.5 Hz
109o
120o
120o
- 2.4 Hz +1.1 Hz
C H
+49.6 Hz
2JHH
180o
2JCH
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H
H(C)
H
C CH(C)
0o 90o 180o
5
10
3J (Hz)
1H, 1H coupling3JHH = 7- cos + 3.83 cos 2
1H, 13C coupling3JCH = 3.81 - 0.9 cos + 3.83 cos 2
Karplus relation
Three-Bond coupling ( Three-Bond coupling ( 33J J ))
3JCH ≈ 0.6 3JHH
H1a
H2a
H2e
3Jaa ≈ 7 - 9 Hz
3Jac ≈ 3Jac ≈ 2 - 5 Hz
HH
H
H
3Jcis ≈ 6 - 14 (10Hz)
3Jtrans ≈ 14-20 (16 Hz)
H3C
H
HC
H
7.5Hz
12.4Hz
7.6Hz
3JCH3JHH
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HH
H H
Long-range coupling (Long-range coupling ( 2+n 2+nJ J ))
allylic coupling
W configuration
H H
H
H
H
Hhomoallylic coupling
+1.1 Hz
-0.3 ~ -3.0 Hz
+0.4 Hz
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11 1
1 2 11 3 3 1
1 4 6 4 1
11stst order spectrum order spectrum
>> J
J(H-Ha) = J(H-Hb) = J(H-Hc)
Pascal Triangle
CH2
J(H-Ha)
J(H-Hb)
J(H-Hc)
O
HH
Hc
Hb
Ha
J(H-Hb)
J(H-Hc) J(H-Hc)
H
HC CH
CH2
A
MR
X
JAR=5Hz,
JAX=6Hz
JAM=8Hz
8 Hz
5 Hz
6 Hz
5 Hz A
5 Hz
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The general two cases below will most likely have 2nd order patterns▪ Aromatic protons chemical shift difference, = 0.1 ~0.5 ppm coupling constant 3JHH = 9.0 Hz, 4JHH = 3.0 Hz, 5JHH = 0.5 Hz
▪ Protons in the restricted environment
22ndnd order spectrum order spectrum
≈ J
1 2 3 4A BZA B
>> J
= 0
A B
A
≈ J
HA OH
HB
HA
Cl HB
Br
S
HA HB
ClBr
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H3C CH3
H3C O
H
H
H
H
H
4-isopropylacetophenone
10 9 8 7 6 5 4 3 2 1 0
a
b
c
e
a
bcd
e
d
220 200 180 160 140 120 100 80 60 40 20 0
C
CC
C
CC
CH3C CH3
CH3C O
H
H
H
H
Ha
b
c
de
fg
h
a
b
c
d
e
f
h
g
CDCl3
1H and 13C spectra for a sample
1H
13C
220 200 180 160 140 120 100 80 60 40 20 0
a
bc
def
g
h
CDCl3
C
CC
C
CC
CH3C CH3
CH3C O
H
H
H
H
H
a
b
c
d
e
f
h
gProton Decoupling